Home / Recalls / Medical Devices
Stryker Medical Division of Stryker Corporation recalls Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Recalled December 21, 2022 · FDA recall Z-0479-2023 · Stryker Medical Division of Stryker
Hazard
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected. · FDA Class II
Units
465 (403 US; 62 OUS)
Sold at
Worldwide Distribution: US (Nationwide) and Foreign to countries of: Australia, Canada, Netherlands, and United Kingdom.
Description
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
Product
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Manufacturer(s)
Stryker Medical Division of Stryker Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →